Häberle H, Velhagen K H, Pleyer U
Augenklinik, Charité und Virchow-Klinikum, Humboldt-Universität zu Berlin.
Ophthalmologe. 1998 Dec;95(12):823-7. doi: 10.1007/s003470050360.
Cataract secondary to juvenile rheumatoid arthritis is a severe, vision-threatening complication in early childhood. Intraocular lens implantation is controversial. The follow-up of four pseudophakic eyes of three patients and their perioperative therapeutic regimen were retrospectively analyzed. Early and late postoperative complications are reported.
Both girls had lens aspiration and posterior lens implantation at the ages of 6 and 12 years, the boy at the age of 10 and 14 years. All patients had relapsing anterior uveitis. The follow-up time was 3 years (1-6 years). One girl was diagnosed with sarcoidosis, causing juvenile arthritis. Both girls had perioperative methothrexate and prednisolone therapy. The boy had azathioprine therapy at the time of his first cataract surgery; later he had no systemic therapy. Both girls' intraocular lenses were implanted at different eye hospitals.
Both girls had severe inflammatory reactions after surgery. At the hospitals both eyes had surgical revision for iris capture. In one case this was combined with exchanging the intraocular lens. Iris capture persisted for this eye and later vitrectomy with silicone oil filling was necessary to delay phthisis, resulting in amaurosis. For two pseudophakic eyes vitrectomy was necessary later because of severe vitreous opacities, but visual acuity was severely diminished by chronic cystoid macular edema and epiretinal membranes. The boy developed in his second eye intermittent iris bombata and persistent secondary glaucoma, visual acuity was stabilized at 0.5.
Secondary cataract due to juvenile rheumatoid arthritis or sarcoidosis is a difficult situation for phacoemulsification with intraocular lens implantation in children. For severe inflammatory complications intense local and systemic anti-inflammatory therapy is mandatory. Visual prognosis is reduced for the uveitic posterior segment and glaucoma complications. IOL implantation can be recommended for only a very few patients.
幼年型类风湿关节炎继发的白内障是儿童早期一种严重的、威胁视力的并发症。人工晶状体植入存在争议。回顾性分析了3例患者4只人工晶状体眼的随访情况及其围手术期治疗方案。报告了术后早期和晚期并发症。
两名女孩分别在6岁和12岁时进行了晶状体抽吸和后房型人工晶状体植入,男孩分别在10岁和14岁时进行。所有患者均有复发性前葡萄膜炎。随访时间为3年(1 - 6年)。一名女孩被诊断为结节病,导致幼年型关节炎。两名女孩围手术期均接受甲氨蝶呤和泼尼松龙治疗。男孩在首次白内障手术时接受硫唑嘌呤治疗;后来未接受全身治疗。两名女孩的人工晶状体在不同的眼科医院植入。
两名女孩术后均出现严重炎症反应。在两家医院,两只眼睛均因虹膜嵌顿进行了手术修复。其中1例同时更换了人工晶状体。该眼虹膜嵌顿持续存在,后来需要进行玻璃体切除术并填充硅油以延缓眼球萎缩,导致失明。另外两只人工晶状体眼后来因严重的玻璃体混浊需要进行玻璃体切除术,但由于慢性黄斑囊样水肿和视网膜前膜,视力严重下降。男孩的第二只眼出现间歇性虹膜膨隆和持续性继发性青光眼,视力稳定在0.5。
幼年型类风湿关节炎或结节病继发的白内障对于儿童白内障超声乳化联合人工晶状体植入来说是一种困难的情况。对于严重的炎症并发症,必须进行强化的局部和全身抗炎治疗。葡萄膜炎性后段病变和青光眼并发症会降低视觉预后。仅能推荐极少数患者进行人工晶状体植入。